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R&D CBC - ST Plus Tripack - Indonesia BPOM Medical Device Registration

R&D CBC - ST Plus Tripack is a medical device registered with Indonesia's BPOM (Badan Pengawas Obat dan Makanan) under Analysis ID AKL 20208719301. The device is manufactured by R&D SYSTEMS, INC. from United States, and is classified as Risk Class Kelas Resiko : B. The authorized representative in Indonesia is PT. DIATRON PROMEDIKA.

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BPOM Registered
Risk Class Kelas Resiko : B
R&D CBC - ST Plus Tripack
Analysis ID: AKL 20208719301

Risk Classification

Kelas Resiko : B

Product Class

Kelas : 2

Manufacturer

R&D SYSTEMS, INC.

Country of Origin

United States

Authorized Representative

PT. DIATRON PROMEDIKA

AR Address

Perkantoran Plaza Pasifik Blok B2/41 Jl. Boulevard Barat Raya, Kelapa Gading

Registration Date

Mar 30, 2021

Expiry Date

Jan 04, 2026

Product Type

Hematological Reagents

Hematology quality control mixture.

Invitro Diagnostics

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